Proteins with Improved Solubility and Methods for Producing and Using Same

ABSTRACT

A method is provided for improving the solubility of proteins, for example, bacterial toxins. In one embodiment, solubility is improved by introducing point mutations that replace cysteine residues capable of forming intermolecular disulfide bonds with other amino acid residues that do not form such bonds. By abrogating the ability of the cysteine residues to form inter-molecular disulfide bonds, aggregation of the protein is reduced, thereby improving the solubility of the protein. In another embodiment, solubility of the protein is improved by producing truncated forms of the protein that express the LHN domain and a fragment of the Hc domain. Proteins made according to the method of the invention are useful, for example, as immunodiagnostic agents and vaccine components.

CROSS REFERENCE TO RELATED APPLICATIONS

The present application claims the benefit of U.S. provisional application Nos. 60/724,274, filed Oct. 7, 2005, and 60/742,900, filed Dec. 7, 2005, the entire disclosures of which are incorporated by reference.

DESCRIPTION OF THE INVENTION

1. Field of the Invention

The present invention relates to methods for producing recombinant proteins that exhibit improved utility and process characteristics, such as solubility, compared to the corresponding native proteins. The invention also relates to proteins made according to the present methods, nucleic acids encoding the proteins, and the use of the proteins for prophylactic and therapeutic applications.

2, Background of the Invention

Proteins produced by organisms, and in particular microorganisms such as bacteria, are of interest because of their potential to serve as immunodiagnostic reagents, therapeutic agents, and vaccine components. Toxins are one group of proteins that have been extensively investigated for those purposes. It is often desirable, if not necessary, to purify proteins to remove contaminating materials that render them unsuitable for those uses. However, some proteins will form aggregates during purification. Aggregates tend to exhibit low solubility and other characteristics that are undesirable, such as low immunogenicity. In some cases, aggregates arise when cysteine residues in the protein of interest form aberrant inter-molecular and/or intra-molecular disulfide bonds.

One family of bacterial toxins of interest as immunodiagnostic reagents, therapeutic agents, and vaccine components are the clostridial neurotoxins, such as those from Clostridium botulinum and Clostridium butyricum. Botulinum neurotoxin (BoNT) is one of the most potent toxins known to man. Its ingestion or inhalation inhibits neurotransmitter release from synaptic vesicles, resulting in neuroparalysis and death. The use of Clostridium botulinum neurotoxins as vaccine components is disclosed in U.S. Pat. No. 5,919,665 to J. A. Williams, which is incorporated by reference into this application. In addition, U.S. Pat. Nos. 6,051,239 to Simpson et al., 6,287,566 to M. T. Dertzbaugh, and 6,461,617 to Shone et al., each of which is incorporated by reference into this application, disclose the use of fragments of clostridial neurotoxin as vaccine components.

Seven serologically distinct forms of clostridial neurotoxin exist: types A, B, C, D, E, F, and G. Full length neurotoxin type E, for example, is designated BoNT/E. Each neurotoxin type shares a common architecture in which a catalytic L-chain (LC, ˜50 kDa) is disulfide linked to a receptor binding and translocating H-chain (HC, ˜100 kDa). The HC polypeptide comprises all or part of two distinct functional domains. The carboxy-terminal half of the HC (˜50 kDa), termed the H_(c) domain, is involved in the high affinity, neurospecific binding of the neurotoxin to cell surface receptors on the target neuron. The amino-terminal half, termed the H_(N) domain (˜50 kDa), mediates the translocation of at least some portion of the neurotoxin across cellular membranes such that the functional activity of the LC is expressed within the target cell. Although the heavy chain is required for BoNT to bind and enter the target cell, it is not toxic by itself.

One particular fragment of interest is the LH_(N) fragment, such as the LH_(N) fragment of neurotoxin E (LH_(N)/E). LH_(N)/E corresponds to the first 845 N-terminal amino acid residues of the full length botulinum (or butyricum) neurotoxin E. It includes the LC and H_(N) domains. During in vivo expression, as well as during purification, both recombinant LH_(N)/E (rLH_(N)/E) and native forms of LH_(N)/E form aggregates having a molecular mass ranging from about 120 kD to several million kD. Often LH_(N)/E aggregates having masses of about 200 kD, 300 kD, 400 kD, 500 kD, 600 kD, 700 kD, and 800 kD are observed. Although aggregated rLH_(N)/E can be recovered from insoluble lysate material by detergent extraction/reductant treatment and further purified (˜90%) by anion exchange (Q Sepharose) and gel filtration (Superdex 200) chromatography, the recovered aggregate has undesirable properties. For example, purified aggregated rLH_(N)/E is recognized in a conformation sensitive ELISA to a much lesser degree (˜5-10-fold) compared to the native BoNT/E control, indicating that conformational epitopes are absent and/or buried within the aggregate. Further, animal efficacy data indicate that immunization with aggregated LH_(N)/E does not protect animals against BoNT/E toxin challenge. Because conformational epitopes are known to play a key role in eliciting protective antibody responses, these results were not totally unexpected.

Different fermentation conditions, for example, slow initial growth, less potent inducers, and/or reduced induction temperatures, as well as different detergent extraction/reductant treatments and denaturation (e.g. urea)/refolding methodologies have been being explored in an effort to produce soluble, non-aggregated or less aggregated LH_(N)/E, but with limited success. Hence, there is a need for protein toxins and toxin subfragments, such as LH_(N)/E, that exhibit little or no aggregation and retain conformational epitopes that permit use of the toxins as immunodiagnostic reagents and vaccine components.

SUMMARY OF THE INVENTION

An object of the invention is to provide a method for reducing or preventing aggregate formation during purification and/or formulation of proteins, such as toxins and toxin fragments.

Another object of the invention is to provide greater batch-to-batch consistency within protein products when characterized by standard methods of protein analysis.

Still another object of the invention is to provide proteins with improved solubility and process characteristics.

Yet another object of the invention is to provide toxin proteins and toxin fragments with improved solubility and process characteristics for use as immunodiagnostic reagents, therapeutic agents, and vaccine components.

Additional objects and advantages of the invention will be set forth in part in the description that follows, and in part will be obvious from the description, or may be learned by practice of the invention. The objects and advantages of the invention will be realized and attained by the compositions and methods particularly pointed out in the appended claims.

To achieve the objects and in accordance with the purpose of the invention, as embodied and broadly described herein, the disclosure describes in one embodiment a recombinant protein comprising at least one point mutation that substitutes a cysteine residue with another amino acid residue, wherein said substitution improves the solubility of the recombinant protein. In some embodiments, the protein is a toxin, such as a bacterial toxin, or a fragment thereof. The toxin may be a neurotoxin or neurotoxin fragment from, for example, Clostridium botulinum or Clostridium butyricum. In certain embodiments, the toxin is a clostridial neurotoxin, such as neurotoxin E, or a fragment thereof, such as an LH_(N)/E fragment.

The disclosure also provides toxin fragments that are more soluble than certain other fragments. For example, in some embodiments, the toxin is a clostridial neurotoxin and the fragment is an LH_(N) fragment that further comprises amino acid sequences from the H_(c) fragment, wherein the resulting LH_(N)+H_(C) fragment is more soluble than the LH_(N) fragment. In certain embodiments, these fragments are recombinant neurotoxin E fragments.

The invention also comprises nucleic acids encoding the recombinant proteins set forth in the disclosure, vectors comprising those nucleic acid sequences, and methods of expressing the encoded proteins in host cells.

In yet other embodiments, the invention encompasses methods used in improving the solubility and process characteristics of the toxin and toxin fragments described in the specification.

The invention further comprises methods of using the disclosed toxin and toxin fragments as therapeutic agents and vaccine components.

Thus, the invention provides the following embodiments.

In one embodiment, then invention provides a recombinant protein comprising at least one point mutation that substitutes a cysteine residue with another amino acid residue, wherein said substitution improves the solubility of the recombinant protein.

In another embodiment, the protein is a toxin or non-toxic derivative of a toxin.

Still other embodiments of the invention encompass a toxin or non-toxic derivative of a toxin that is of bacterial origin.

In other embodiments, the bacterial toxin or toxin derivative is from either Clostridium botulinum or Clostridium butyricum.

In yet other embodiments, the toxin is a neurotoxin or neurotoxin derivative.

In still other embodiments, the neurotoxin is neurotoxin A, B, C, D, E, F, or G, or a non-toxic derivative thereof.

In yet other embodiments, the neurotoxin or non-toxic derivative is a fragment of neurotoxin E.

In other embodiments the fragment is the LH_(N)/E fragment of neurotoxin E.

In still other embodiments, the neurotoxin E fragment comprises at least one cysteine to serine amino acid substitution.

In yet other embodiments, the substitution of serine for cysteine occurs at amino acid residue 26, amino acid residue 347, or both amino acid residue 26 and amino acid residue 347 compared to the LH_(N) fragment of SEQ ID NO: 1 or SEQ ID NO: 2.

The invention includes embodiments in which a protein of the invention has active endopeptidase activity.

The invention also includes embodiments in which a protein of the invention has attenuated endopeptidase activity.

Among other embodiments, the invention also includes nucleic acids encoding a recombinant protein of the invention.

Similarly, other embodiments of the invention include a method for improving the solubility of a protein having at least one cysteine residue, that forms an intermolecular disulfide bond, comprising:

-   -   (a) providing a nucleic acid sequence encoding a recombinant         protein comprising at least one cysteine residue;     -   (b) introducing at least one point mutation into the nucleic         acid sequence that substitutes at least one cysteine residue         with another amino acid residue;     -   (c) transforming a host cell with the mutated nucleic acid         sequence; and     -   (d) expressing the nucleic acid sequence to produce the protein.

In some embodiments, the protein in the method is a toxin or non-toxic derivative thereof.

In other embodiments, the protein in the method is a toxin or non-toxic derivative of bacterial origin.

In yet other embodiments, the protein in the method is a bacterial toxin or toxin derivative from either Clostridium botulinum or Clostridium butyricum.

In still other embodiments, the protein in the method is a toxin a neurotoxin or neurotoxin derivative.

In some embodiments, the neurotoxin in the method is neurotoxin A, B, C, D, E, F, or G, or a non-toxic derivative thereof.

In other embodiments, the non-toxic derivative in the method is a is a fragment of neurotoxin E.

In yet other embodiments, the fragment in the method is the LH_(N)/E fragment of neurotoxin E.

In some embodiments of the method, the amino acid introduced by the at least one point mutation is a serine.

In other embodiments of the method, the protein is a LH_(N) fragment of clostridial neurotoxin E and the at least one point mutation substitutes a serine for a cysteine at amino acid residue 26, amino acid residue 347, or both amino acid residue 26 and amino acid residue 347 compared to the LH_(N) fragment of SEQ ID NO: 1 or SEQ ID NO: 2.

In still other embodiments of the method, the point mutation is introduced by site-directed mutagenesis.

Various embodiments of the method further comprise isolating the protein.

In certain embodiments of the method, the host cell is a mammalian, plant, insect, fungal, or bacterial cell.

The methods of the invention include embodiments in which a protein of the invention has active endopeptidase activity.

The methods of the invention also include embodiments in which a protein of the invention has attenuated endopeptidase activity.

In some embodiments, the invention provides for the use of a protein of the invention for the manufacture of a medicament for the treatment or prevention of botulism.

Other embodiments of the invention include compositions comprising a protein of the invention and a pharmaceutically acceptable carrier.

In still other embodiments, the invention provides methods of protecting an individual from botulism, comprising administering to the individual a composition of the invention.

Yet other embodiments of the invention provide a method of producing antibodies that neutralize a clostridial neurotoxin, comprising administering a composition of the invention to an animal, allowing the animal to develop neutralizing antibodies to the clostridial neurotoxin, and isolating an antiserum that neutralizes the clostridial neurotoxin from the animal.

Other embodiments encompass an antiserum produced by a method of the invention.

In still other embodiments, the invention provides methods of treating exposure to a clostridial neurotoxin, comprising administering to a patient that has been exposed to the clostridial neurotoxin an antiserum of the invention.

In other embodiments, the invention provides a recombinant protein comprising a truncated botulinum serotype E toxin wherein the truncation improves the solubility of the recombinant protein.

In some embodiments, the protein comprises a truncation in the Hc domain.

In other embodiments, the truncated protein comprises the LH_(N)/E domain and the amino terminal 103 amino acids of the Hc domain.

Still other embodiments of the invention encompass a truncated protein comprising the amino terminal 948 amino acids of the serotype E toxin.

In yet other embodiments, the truncated protein comprises the LH_(N)/E domain and the amino terminal 202 amino acids of the Hc domain.

Still other embodiments of the invention encompass a truncated protein comprising the amino terminal 1047 amino acids of the serotype E toxin.

In other embodiments, the truncated protein comprises the LH_(N)/E domain and the amino terminal 304 amino acids of the Hc domain.

Still other embodiments of the invention encompass a truncated protein comprising the amino terminal 1149 amino acids of the serotype E toxin.

Additional embodiments of the invention include nucleic acids encoding a truncated botulinum serotype E toxin.

In still other embodiments, the invention provides methods for improving the solubility of a clostridial neurotoxin, comprising:

-   -   (a) providing a nucleic acid sequence encoding clostridial         neurotoxin;     -   (b) modifying the nucleic acid sequence so that it encodes the         LH_(N) fragment and a portion of the H_(c) fragment of the         neurotoxin;     -   (c) transforming the modified nucleic acid sequence into a host         cell capable of expressing the modified nucleic acid sequence;         and     -   (d) expressing the modified nucleic acid sequence to produce the         protein.

In yet other embodiments, the invention provides for use of a truncated botulinum serotype E toxin for the manufacture of a medicament for the treatment or prevention of botulism.

In other embodiments, the invention provides a composition comprising a truncated botulinum serotype E toxin and a pharmaceutically acceptable carrier.

In still other embodiments, the invention provides a method of protecting an individual from botulism, comprising administering to the individual a composition comprising a truncated botulinum serotype E toxin and a pharmaceutically acceptable carrier.

Other embodiments of the invention include a method of producing antibodies that neutralize a clostridial neurotoxin, comprising administering a composition comprising a truncated botulinum serotype E toxin and a pharmaceutically acceptable carrier to an animal, allowing the animal to develop neutralizing antibodies to the clostridial neurotoxin, and isolating an antiserum that neutralizes the clostridial neurotoxin from the animal.

In still other embodiments, the invention provides an antiserum produced by the method of the preceding paragraph.

In yet other embodiment, the invention provides methods of treating exposure to a clostridial neurotoxin, comprising administering to a patient that has been exposed to the clostridial neurotoxin an antiserum of the invention.

In yet another embodiment, the invention provides a mutated botulinum serotype E toxin comprising either or both of a leucine residue substituted for the tryptophan residue at position 1223 and a phenylalanine residue for the tyrosine residue at position 1224 of SEQ ID NO: 1 or SEQ ID NO: 2.

The invention also provides, in additional embodiments, for the use of a protein of the preceding paragraph for the manufacture of a medicament for the treatment or prevention of botulism.

In still other embodiments, the invention provides an in vitro method for improving the solubility of a protein having at least one cysteine residue that forms an intermolecular disulfide bond, comprising:

-   -   (a) providing a nucleic acid sequence encoding a recombinant         protein comprising at least one cysteine residue;     -   (b) introducing at least one point mutation into the nucleic         acid sequence that substitutes at least one cysteine residue         with another amino acid residue;     -   (c) transforming a host cell with the mutated nucleic acid         sequence; and     -   (d) expressing the nucleic acid sequence to produce the protein.

Yet other embodiments of the invention encompass an in vitro method for improving the solubility of a clostridial neurotoxin, comprising:

-   -   (a) providing a nucleic acid sequence encoding a clostridial         neurotoxin;     -   (b) modifying the nucleic acid sequence so that it encodes the         LH_(N) fragment and a portion of the H_(c) fragment of the         neurotoxin;     -   (c) transforming the modified nucleic acid sequence into a host         cell capable of expressing the modified nucleic acid sequence;         and     -   (d) expressing the modified nucleic acid sequence to produce the         protein.

In still other embodiments, the invention provides a method of producing antibodies that neutralize a clostridial neurotoxin, comprising isolating antibodies elicited by an inoculated polypeptide, wherein said polypeptide is a protein according to the invention.

Yet other embodiments of the invention provided for the use of an antiserum of the invention for the manufacture of a medicament for treating exposure to clostridial neurotoxin.

It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory only and are not restrictive of the invention, as claimed. The accompanying drawings illustrate embodiments of the invention and together with the description, serve to explain the principles of the invention.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1A and 1B are a polyacrylamide gel and chromatogram, respectively, showing production of recombinant LH_(N)/E in Escherichia coli as a high molecular weight aggregate.

FIGS. 2A and 2B demonstrate high levels of mutated recombinant LH_(N)/E in Escherichia coli as non-aggregated proteins.

FIGS. 3A and 3B are Coomassie Blue stained gels demonstrating that the solubility of the LH_(N)/E-Hc protein increases as the length of the Hc sequence included in the protein increases.

FIGS. 4A and 4B are western blots demonstrating that the solubility of the LH_(N)/E-Hc protein increases as the length of the Hc sequence included in the protein increases.

FIGS. 5A and 5B are a Coomassie Blue stained gel and western blot analysis, respectively, of the solubility of the LH_(N)/E and LH_(N)/E-H_(c)406 proteins in the presence of the reducing agent DTT.

FIG. 6 is a western blot comparing protein levels in total lysate, the soluble fraction, and the insoluble fraction for LH_(N) proteins comprising Cys to Ser replacements at positions 26 and 347, and having or lacking an Hc fragment.

DESCRIPTION OF THE EMBODIMENTS

The section headings used herein are for organizational purposes only and are not to be construed as limiting the subject matter described. All documents, or portions of documents, cited herein, including but not limited to patents, patent applications, articles, books, and treatises, are hereby expressly incorporated by reference in their entirety for any purpose. In the event that one or more of the incorporated documents or portions of documents defines a term that contradicts that term's definition in the application, this application controls.

The use of the singular includes the plural unless specifically stated otherwise. The word “a” or “an” means “at least one” unless specifically stated otherwise. The use of “or” means “and/or” unless stated otherwise. The meaning of the phrase “at least one” is equivalent to the meaning of the phrase “one or more.” Furthermore, the use of the term “including,” as well as other forms, such as “includes” and “included,” is not limiting. Also, terms such as “element” or “component” encompass both elements or components comprising one unit and elements or components comprising more than one unit unless specifically stated otherwise.

Neurotoxic proteins and fragments of these proteins are important immunodiagnostic reagents, therapeutic agents, and vaccine components. Functional neurotoxins are hazardous to work with, however, so investigators prefer to use recombinant proteins that have been genetically modified to reduce or eliminate their neurotoxicity. Unfortunately, it can be difficult to purify some of the recombinant, non-toxic, proteins because they often form aggregates, which have reduced solubility and are less effective reagents for use in immunodiagnostic, therapeutic, and vaccine applications. For example, although aggregated rLH_(N)/E can be purified, it is recognized in a conformation-sensitive ELISA to a much lesser degree (˜5-10-fold) than is the native BoNT/E toxin, indicating that conformational epitopes are absent and/or buried within the aggregate. Also, immunization with aggregated LH_(N)/E does not protect animals against BoNT/E toxin challenge.

Accordingly, the disclosure provides recombinant proteins with improved solubility. For example, in one embodiment, the disclosure describes a recombinant protein comprising at least one point mutation that substitutes, a cysteine residue with another amino acid residue, wherein said substitution improves the solubility of the recombinant protein. In some embodiments, the protein is a toxin, such as a bacterial toxin, for example, a neurotoxin or neurotoxin fragment from Clostridium botulinum or Clostridium butyricum. In some embodiments, the protein is a fragment of a neurotoxin, such as an LH_(N) fragment, for example, an LH_(N)/E fragment. In certain embodiments, the first and third cysteine residues, counting from the amino terminus of a naturally-occurring neurotoxin amino acid sequence, have been replaced with non-cysteine amino acids, such as serine, in the recombinant neurotoxin protein or fragment thereof. Although mutations in clostridial neurotoxin E are exemplified, clostridial neurotoxins A, B, C, D, F, and G can be modified in the same manner.

Nucleic acid sequences encoding various neurotoxins have been cloned and those nucleic acid sequences are known in the art. For example, a nucleic acid sequence of a full length neurotoxin E from C. botulinum is provided in GenBank accession no. AB082519. A nucleic acid sequence of a full length neurotoxin E from C. butyricum is provided in GenBank accession no. AB088207.

An example of an amino acid sequence of C. botulinum BoNT/E neurotoxin is:

(SEQ ID NO: 1) MPKINSFNYN DPVNDRTILY IKPGGCQEFY KSFNIMKNIW IIPERNVIGT TPQDFHPPTS LKNGDSSYYD PNYLQSDEEK DRFLKIVTKI FNRINNNLSG GILLEELSKA NPYLGNDNTP DNQFHIGDAS AVEIKFSNGS QDILLPNVII MGAEPDLFET NSSNISLRNN YMPSNHRFGS IAIVTFSPEY SFRFNDNCMN EFIQDPALTL MHELINSLHG LYGAKGITTK YTITQKQNPL ITNIRGTNIE EFLTFGGTDL NIITSAQSND IYTNLLADYK KIASKLSKVQ VSNPLLNPYK DVFEAKYGLD KDASGIYSVN INKFNDIFKK LYSFTEFDLR TKFQVKCRQT YIGQYKYFKL SNLLNDSIYN ISEGYNINNL KVNFRGQNAN LNPRIITPIT GRGLVKKIIR FCKNIVSVKG IRKSICIEIN NGELFFVASE NSYNDDNINT PKEIDDTVTS NNNYENDLDQ VILNFNSESA PGLSDEKLNL TIQNDAYIPK YDSNGTSDIE QHDVNELNVF FYLDAQKVPE GENNVNLTSS IDTALLEQPK IYTFFSSEFI NNVNKPVQAA LFVSWIQQVL VDFTTEANQK STVDKIADIS IVVPYIGLAL NIGNEAQKGN FKDALELLGA GILLEFEPEL LIPTILVFTI KSFLGSSDNK NKVIKAINNA LKERDEKWKE VYSFIVSNWM TKINTQFNKR KEQMYQALQN QVNAIKTIIE SKYNSYTLEE KNELTNKYDI KQIENELNQK VSIAMNNIDR FLTESSISYL MKIINEVKIN KLREYDENVK TYLLNYIIQH GSILGESQQE LNSMVTDTLN NSIPFKLSSY TDDKILISYF NKFFKRIKSS SVLNMRYKND KYVDTSGYDS NININGDVYK YPTNKNQFGI YNDKLSEVNI SQNDYIIYDN KYKNFSISFW VRIPNYDNKI VNVNNEYTII NCMRDNNSGW KVSLNHNEII WTFEDNRGIN QKLAFNYGNA NGISDYINKW IFVTITNDRL GDSKLYINGN LIDQKSILNL GNIHVSDNIL FKIVNCSYTR YIGIRYFNIF DKELDETEIQ TLYSNEPNTN ILKDFWGNYL LYDKEYYLLN VLKPNNFIDR RKDSTLSINN IRSTILLANR LYSGIKVKIQ RVNNSSTNDN LVRKNDQVYI NFVASKTHLF PLYADTATTN KEKTIKISSS GNRFNQVVVM NSVGNCTMNF KNNNGNNIGL LGFKADTVVA STWYYTHMRD HTNSNGCFWN FISEEHGWQE K.

This sequence includes the Met at residue 1. SEQ ID NO: 1 is the reference sequence for all numbering regarding C. botulinum BoNT/E and fragments thereof used in this specification, irrespective of whether those sequences have or do not have the first Met. The LH_(N)/E fragment extends from the amino terminus to amino acid residue 845 (Lys) in SEQ ID NO: 1.

An example of an amino acid sequence of C. butryicum BoNT/E neurotoxin is:

(SEQ ID NO: 2) MPTINSFNYN DPVNNRTILY IKPGGCQQFY KSFNIMKNIW IIPERNVIGT IPQDFLPPTS LKNGDSSYYD PNYLQSDQEK DKFLKIVTKI FNRINDNLSG RILLEELSKA NPYLGNDNTP DGDFIINDAS AVPIQFSNGS QSILLPNVII MGAEPDLFET NSSNISLRNN YMPSNHGFGS IAIVTFSPEY SFRFKDNSMN EFIQDPALTL MHELIHSLHG LYGAKGITTK YTITQKQNPL ITNIRGTNIE EFLTFGGTDL NIITSAQSND IYTNLLADYK KIASKLSKVQ VSNPLLNPYK DVFEAKYGLD KDASGIYSVN INKFNDIFKK LYSFTEFDLA TKFQVKCRQT YIGQYKYFKL SNLLNDSIYN ISEGYNINNL KVNFRGQNAN LNPRIITPIT GRGLVKKIIR FCKNIVSVKG IRKSICIEIN NGELFFVASE NSYNDDNINT PKEIDDTVTS NNNYENDLDQ VILNFNSESA PGLSDEKLNL TIQNDAYIPK YDSNGTSDIE QHDVNELNVF FYLDAQKVPE GENNVNLTSS IDTALLEQPK IYTFFSSEFI NNVNKPVQAA LFVGWIQQVL VDFTTEANQK STVDKIADIS IVVPYIGLAL NIGNEAQKGN FKDALELLGA GILLEFEPEL LIPTILVFTI KSFLGSSDNK NKVIKAINNA LKERDEKWKE VYSFIVSNWM TKINTQFNKR KEQMYQALQN QVNALKAIIE SKYNSYTLEE KNELTNKYDI EQIENELNQK VSIAMNNIDR FLTESSISYL MKLINEVKIN KLREYDENVK TYLLDYIIKH GSILGESQQE LNSMVIDTLN NSIPFKLSSY TDDKILISYF NKFFKRIKSS SVLNNRYKND KYVDTSGYDS NININGDVYK YPTNKNQFGI YNDKLSEVNI SQNDYIIYDN KYKNFSISFW VRIPNYDNKI VNVNNEYTII NCMRDNNSGW KVSLNHNEII WTLQDNSGIN QKLAFNYGNA NGISDYINKW IFVTITNDRL GDSKLYINGN LIDKKSILNL GNIHVSDNIL FKIVNCSYTR YIGIRYFNIF DKELDETEIQ TLYNNEPNAN ILKDFWGNYL LYDKEYYLLN VLKPNNFINR RTDSTLSINN IRSTILLANR LYSGIKVKIQ RVNNSSTNDN LVRKNDQVYI NFVASKTHLL PLYADTATTN KEKTIKISSS GNRFNQVVVM NSVGNCTMNF KNNNGNNIGL LGFKADTVVA STWYYTHMRD NTNSNGFFWN FISEEHGWQE K.

This sequence includes the Met at residue 1. SEQ ID NO: 2 is the reference sequence for all numbering-regarding C. butyricum BoNT/E and fragments thereof used in this specification, irrespective of whether those sequences have or do not have the first Met. The LH_(N)/E fragment extends from the amino terminus to amino acid residue 845 (Lys) in SEQ ID NO: 2.

In the case of neurotoxin proteins from C. botulinum and C. butyricum, any amino acid sequences disclosed in which the initial methionine is not included are also considered BoNT/E or LH_(N)/E fragments, as appropriate, even though the numbering of the amino acid residues in that particular fragment assumes the Met at position 1.

BoNT/E and fragments thereof that have endopeptidase activity have a glutamate (E) at position 213 and a histidine (H) at position 216. The endopeptidase activity can be abolished by mutating these sequences. For example, the specification describes BoNT/E and fragments thereof in which the glutamate is replaced with glutamine (Q) (i.e., E213Q) and the histidine is replaced with a tyrosine (Y) (i.e., H216Y). These proteins lack endopeptidase activity.

Examples of recombinant proteins comprising at least one point mutation that substitutes a cysteine residue with another amino acid residue, wherein said substitution improves the solubility of the recombinant protein include, but are not limited to:

-   -   a) a protein comprising residues 2 to 845 of the amino acid         sequence set forth in SEQ ID NO: 1, wherein the cysteine at         position 26 of SEQ ID NO: 1 is replaced with a serine;     -   b) a protein comprising residues 2 to 845 of the amino acid         sequence set forth in SEQ ID NO: 1, wherein the cysteine at         position 347 of SEQ ID NO: 1 is replaced with a serine;     -   c) a protein comprising residues 2 to 845 of the amino acid         sequence set forth in SEQ ID NO: 1, wherein the cysteine at         position 26 and the cysteine at position 347 of SEQ ID NO: 1 are         each replaced with a serine;     -   d) a protein comprising residues 2 to 845 of the amino acid         sequence set forth in SEQ ID NO: 2, wherein the cysteine at         position 26 of SEQ ID NO: 2 is replaced with a serine;     -   e) a protein comprising residues 2 to 845 of the amino acid         sequence set forth in SEQ ID NO: 2, wherein the cysteine at         position 347 of SEQ ID NO: 2 is replaced with a serine; and     -   f) a protein comprising residues 2 to 845 of the amino acid         sequence set forth in SEQ ID NO: 2, wherein the cysteine at         position 26 and the cysteine at position 347 of SEQ ID NO: 2 are         each replaced with a serine.

In alternative embodiments, each of the proteins described in parts (a)-(f) of the preceding paragraph may consist of, rather than comprise, the respective amino acid sequences. Optionally, each of the proteins described in parts (a)-(f) of the preceding paragraph may further comprise a methionine at their respective amino termini. The solubility, immunogenicity, or both solubility and immunogenicity of the proteins described in parts (a)-(f) of the preceding paragraph is improved compared to proteins comprising or consisting of the corresponding amino acid sequence lacking the mentioned cysteine to serine replacement(s). In some embodiments, the proteins contain the E213Q and H216Y point mutations that abolish endopeptidase activity.

Additional examples of BoNT/E proteins or fragments thereof comprising Cys to Ser replacements are set forth in SEQ ID NOS: 7-14.

The disclosure also provides recombinant neurotoxins fragments that are more soluble than certain other fragments. For example, in some embodiments, the fragment is an LH_(N) fragment that further comprises amino acid sequences from the H_(c) fragment, wherein the resulting LH_(N)+H_(c) fragment is more soluble than the LH_(N) fragment. In certain embodiments, the LH_(N) fragment is an LH_(N)/E fragment and the H_(c) fragment is an H_(c)/E fragment. The LH_(N) fragment may optionally comprise at least one point mutation that substitutes a cysteine residue with another amino acid residue.

Examples of recombinant neurotoxins fragments that are more soluble than certain other fragments include, but are not limited to:

-   -   a) a protein comprising residues 2 to 948 of the amino acid         sequence set forth in SEQ ID NO: 1;     -   b) a protein comprising residues 2 to 1047 of the amino acid         sequence set forth in SEQ ID NO: 1;     -   c) a protein comprising residues 2 to 1149 of the amino acid         sequence set forth in SEQ ID NO: 1;     -   d) a protein comprising residues 2 to 948 of the amino acid         sequence set forth in SEQ ID NO: 2;     -   e) a protein comprising residues 2 to 1047 of the amino acid         sequence set forth in SEQ ID NO: 2; and     -   f) a protein comprising residues 2 to 1149 of the amino acid         sequence set forth in SEQ ID NO: 2.

In alternative embodiments, each of the proteins described in parts (a)-(f) of the preceding paragraph may consist of, rather than comprise, the respective amino acid sequences. Optionally, each of the proteins described in parts (a)-(f) of the preceding paragraph may further comprise a methionine at their respective amino terminus. The proteins described in parts (a)-(f) of the preceding paragraph may also optionally comprise a Cys to Ser substitution at amino acid residue 26, 347, or 26 and 347 of SEQ ID NO: 1, or SEQ ID NO: 2, as appropriate. The solubility, immunogenicity, or both solubility and immunogenicity of the proteins described in parts (a)-(f) of the preceding paragraph is improved compared to proteins consisting of amino acids 2-845 of the corresponding amino acid sequence. That is, the proteins described in parts (a)-(f) of the preceding paragraph have improved solubility, improved immunogenicity, or improved solubility and improved immunogenicity compared to the LH_(N) fragment of SEQ ID NO: 1 or SEQ ID NO: 2. In some embodiments, the proteins contain the E213Q and H216Y point mutations that abolish endopeptidase activity.

Additional examples of proteins comprising an extended LH_(N) fragment are set forth in SEQ ID NO: 10 and SEQ ID NO: 14. Expression constructs LH_(N)/E-Hc103; LH_(N)/E-Hc202; LH_(N)/E-Hc304; and LH_(N)/E-Hc406 also contain nucleic acid sequences encoding proteins comprising an extended LH_(N) fragment.

Proteins that comprise amino acid residues 1223 or 1224 (relative to SEQ ID NO: 1 or SEQ ID NO: 2) of neurotoxin E may further comprise an amino acid substitution at either residue 1223, residue 1224, or both residue 1223 and 1224. For example, the protein may comprise a tryptophan (W) to leucine (L) mutation at positions 1223 (i.e., W1223L), a tyrosine (Y) to phenylalanine (F) mutation at position 1224 (i.e., Y1224F), or a W1223L and a Y1224F double mutation. Examples of protein comprising these mutations are set forth in SEQ ID NO: 9 and SEQ ID NO: 13.

The invention also comprises nucleic acids encoding the various recombinant proteins described in the specification, vectors comprising those nucleic acid sequences, and methods of expressing the encoded protein in a host cell. Thus, in some embodiments, the nucleic acids encode modified C. botulinum or C. butyricum neurotoxins, such as neurotoxin E, or fragments thereof, such as an LH_(N) fragment, that have improved solubility, immunogenicity, or both improved solubility and immunogenicity compared to the corresponding unmodified neurotoxin or neurotoxin fragment. Methods of measuring solubility and immunogenicity are known in the art, and include, but are not limited to, the methods described in the Examples.

An improvement in solubility can be accomplished by changing codons in the nucleic acid sequence that code for the amino acid cysteine to another amino acid that does not form a disulfide bond. Alternatively, or in addition, solubility can be improved by extending the sequence of a fragment, such as an LH_(N) fragment of a clostridial neurotoxin, by providing additional sequences from an adjoining segment, such as an H_(c) fragment of a clostridial neurotoxin.

Methods of manipulating nucleic acids and of expressing the encoded proteins are known in the art, and include those described in Molecular Cloning, A Laboratory Manual (2nd Ed., Sambrook, Fritsch and Maniatis, Cold Spring Harbor) and Current Protocols in Molecular Biology (Eds. Aufubel, Brent, Kingston, More, Feidman, Smith and Stuhl. Greene Publ. Assoc., Wiley-Interscience, N.Y., 1992). Thus, it is possible to modify a nucleic acid sequence by replacing the codon for cysteine with a codon for another amino acid. In general, a cysteine is replaced with a serine, but other amino acid substitutions are also possible, such as replacement of cysteine with alanine, glycine, valine, leucine, isoleucine, or modified forms of these amino acids, so long as the replacement amino acid does not readily form disulfide bonds. Alternatively, the cysteine residue may simply be deleted from the sequence. Obviously, a deletion must remove the codon for the cysteine from the nucleic acid sequence without introducing a frameshift. Techniques for making substitution and deletion mutations at predetermined sites in a nucleic acid having a known sequence are well known and include, but are not limited to, primer mutagenesis and other forms of site-directed mutagenesis.

Similarly, methods of joining two sequence fragments, such as an LH_(N) and an H_(c) fragment of a clostridial neurotoxin, and of truncating a sequence, are known in the art. These include, but are not limited to, PCR-based techniques and techniques for ligating together two or more nucleic acid sequences.

Certain methods of expressing proteins are described in the Examples. Other methods can also be used, however. Generally, in order to express a protein, such as a bacterial toxin or fragment thereof, a suitable cell line is transformed with a DNA sequence encoding that protein under the control of known regulatory sequences. The transformed host cells are cultured and the protein recovered and isolated from the culture medium. The isolated expressed proteins are substantially free from other proteins with which they are co-produced as well as from other contaminants. Suitable cells or cell lines may be mammalian cells, such as Chinese hamster ovary cells (CHO), the monkey kidney COS-1 cell line, or mammalian CV-1 cells. The selection of suitable mammalian host cells and methods for transformation, culturing, amplification, screening, product production and purification are known in the art. (See, e.g., Gething and Sambrook, Nature, 293:620-625 (1981); Kaufman et al., Mol Cell Biol., 5(7):1750-1759 (1985); Howley et al., U.S. Pat. No. 4,419,446.))

Bacterial cells may also be used as suitable hosts for expression of a bacterial toxin or fragment thereof. For example, various strains of E. coli (e.g., HB101, MC1061) are well-known as host cells in the field of biotechnology. Various strains of B. subtilis, Pseudomonas, other bacilli and the like may also be used. For expression of a protein in bacterial cells, DNA encoding the propeptide is generally not necessary.

In some embodiments, the bacterial toxin or fragment thereof is expressed using a vector that contains a DNA sequence encoding the protein and appropriate expression control sequences. Expression control sequences for such vectors are known to those skilled in the art and may be selected depending upon the host cells. In other embodiments, the bacterial toxin or fragment thereof is expressed as a fusion protein comprising the protein sequence of the bacterial toxin or fragment thereof and, for example, a tag to stabilize the resulting fusion protein or to simplify purification of the bacterial toxin or fragment thereof. Such tags are known in the art. Representative examples include sequences which encode a series of histidine residues, the epitope tag FLAG, the Herpes simplex glycoprotein D, beta-galactosidase, maltose binding protein, streptavidin tag or glutathione S-transferase.

The invention also encompasses the methods used for improving the solubility and process characteristics of a protein. For example, in some embodiments, the disclosure provides methods for improving the solubility and process characteristics of a protein having at least one cysteine residue that forms an intermolecular disulfide bond, comprising:

-   -   (a) providing a nucleic acid sequence encoding a recombinant         protein comprising at least one cysteine residue;     -   (b) introducing at least one point mutation into the nucleic         acid sequence that substitutes at least one cysteine residue         with another amino acid residue;     -   (c) transforming a host cell with the mutated nucleic acid         sequence; and     -   (d) expressing the nucleic acid sequence to produce the protein.

In other embodiments, the method comprises improving the solubility of a botulinum neurotoxin, comprising:

-   -   (a) providing a nucleic acid sequence encoding a botulinum         neurotoxin;     -   (b) modifying the nucleic acid sequence so that it encodes the         LHN fragment and a portion of the H_(c) fragment of the         neurotoxin;     -   (c) transforming the modified nucleic acid sequence into a host         cell capable of expressing the modified nucleic acid sequence;         and     -   (d) expressing the modified nucleic acid sequence to produce the         protein.

The methods for improving the solubility of a protein, such as a botulinum neurotoxin, can be entirely in vitro methods. In other embodiments, as discussed herein, the methods can include an in vivo aspect, such expressing the nucleic acid in vivo.

Unless otherwise stated, a “soluble” recombinant protein is one that is exists in solution in the cytoplasm of the host cell. If the protein contains a signal sequence the soluble protein is exported to the periplasmic space in bacteria hosts and is secreted into the culture medium in eukaryotic cells capable of secretion or by bacterial host possessing the appropriate genes. In contrast, an insoluble protein is one which exists in denatured form inside cytoplasmic granules (called an inclusion bodies) in the host cell. A soluble protein is a protein which is not found in an inclusion body inside the host cell or is found both in the cytoplasm and in inclusion bodies and in this case the protein may be present at high or low levels in the cytoplasm.

A soluble protein is distinct from a “solubilized” protein. An insoluble recombinant protein found inside an inclusion body may be solubilized (i.e., rendered into a soluble form) by treating purified inclusion bodies with denaturants such as guanidine hydrochloride, urea or sodium dodecyl sulfate (SDS). These denaturants must then be removed from the solubilized protein preparation to allow the recovered protein to renature (refold). A distinction is also made between proteins that are soluble (i.e., dissolved) in a solution devoid of significant amounts of ionic detergents (e.g., SDS) or denaturants (e.g., urea, guanidine hydrochloride) and proteins that exist as a suspension of insoluble protein molecules dispersed within the solution. A soluble protein will not be removed from a solution containing the protein by centrifugation using conditions sufficient to remove bacteria present in a liquid medium (e.g., centrifugation at 5,000 g for 4-5 minutes). A method of testing whether a protein is soluble or insoluble is described in U.S. Pat. No. 5,919,665, which is incorporated by reference.

The invention further encompasses methods of using the disclosed toxin and toxin fragments as therapeutic agents and vaccine components. Optionally, the disclosed toxin and toxin fragments are tested to ensure that they are free or substantially free of endotoxin activity. Methods of testing for endotoxin activity are known in the art.

Toxins and toxin fragments useful in vaccine compositions are those that can stimulate an antibody response that neutralizes a wild-type toxin of the same type. For example, when the toxin or toxin fragment is derived from clostridial type E neurotoxin, then the toxin or toxin fragment composition stimulates antibodies that neutralize the toxin activity of wild-type BoNT/E. By way of example only, one method for selecting clostridial neurotoxin toxins or neurotoxin fragments that can stimulate an antibody response that neutralizes wild-type BoNT activity is to determine whether the clostridial neurotoxin or neurotoxin fragment is immunoreactive with polyclonal neutralizing antibodies to wild-type BoNT of same type, such as BoNT/E. Methods of determining whether clostridial neurotoxin or neurotoxin fragment immunoreact with antibodies to wild-type BoNT include ELISA, western blot, double immunodiffusion assay, RIA, and the like. Another exemplary method comprises using the clostridial neurotoxin or neurotoxin fragments as an immunogen in mice, then determining whether the mice are protected from challenge with wild-type BoNT, such as wild-type BoNT/E.

A toxin or toxin fragment can be combined with a pharmaceutically acceptable carrier. Physiologically acceptable diluents include physiological saline solutions, and buffered saline solutions at neutral pH such as phosphate buffered saline. Other types of physiological carriers include liposomes and polymers. Optionally, the toxin or toxin fragments can be combined with an adjuvant. In some embodiments, the adjuvant is IC31™, produced by Intercell AG, Vienna, Austria. (See EP 1 326 634B and EP 1 296 713B.) In other embodiments, the adjuvant is a Toll-like receptor (TLR) agonist, such as a TLR 4 agonist, a TLR7 agonist, or a TLR9 agonist. TLR9 agonists include, for example, immunostimulatory CpG nucleic acid sequences. Other examples of adjuvants that can be used include, but are not limited to, Freund's incomplete adjuvant, Freund's complete adjuvant, alum, monophosphoryl lipid A, alum phosphate or hydroxide, and QS-21.

For vaccine formulations, the toxins or toxin fragments can also be combined with immunomodulators, such as interleukins and interferons, for example IL-1, IL-12, and IFN-γ.

When the toxin or toxin fragment is a clostridial neurotoxin or neurotoxin fragment, multiple types of clostridial neurotoxin or neurotoxin fragments can be used together in a formulation, or a single type can be used alone. Thus, vaccine formulations and compositions include, but are not limited to, BoNT/E or a fragment of BoNT/E, such as LH_(N)/E, including LH_(N)/E that is mutated and LH_(N)/E that is extended by the inclusion of amino acid sequences from the H_(c) fragments, either alone or in combination with wild-type, mutant, or fragments of one or more of clostridial neurotoxins type A, B, C, D, F, or G. Many vaccine formulations are known to those of skill in the art.

The toxin or toxin fragment is added to a vaccine formulation in an amount effective to stimulate a protective immune response in an animal challenged with wild-type toxin. Thus, in preparing a vaccine formulation, the toxin or toxin fragment is used for the manufacture of a medicament for the treatment or prevention of botulism. Generation of protective antibodies that neutralize the wild-type toxin can be measured by testing the ability of the vaccine to protect an animal, such as a mouse, from challenge with a lethal dose of wild-type toxin. The amounts of the toxin or toxin fragment in the vaccine composition that can form a protective immune response are generally about 0.1 μg to 100 mg per kg of body weight. In some cases, about 1 μg to about 1 mg/kg body weight is used. Often, about 1 μg to about 100 μg toxin or toxin fragment per kg of body weight will be sufficient to stimulate a protective immune response, such as protective antibodies. An amount of toxin or toxin fragment that stimulates a protective immune response is considered to be an “effective amount.”

Depending upon the circumstances, such as the animal to be vaccinated, either a single or multiple doses of the vaccine composition are administered to provide protective immunity against the wild-type toxin. The vaccine composition can be administered to an animal in a variety of ways, including subcutaneously, intramuscularly, intravenously, intradermally, orally, intranasally, ocularly, and intraperitoneally.

Any animal that is susceptible to the wild-type toxin can be vaccinated with the toxin or toxin fragment in an immunostimulatory composition. Examples of animals susceptible to clostridial neurotoxins include, but are not limited to, rabbits, rodents, birds, horses, cattle, and humans. Accordingly, a vaccine composition comprising a clostridial neurotoxin or neurotoxin fragment, such as the clostridial neurotoxins and neurotoxin fragments described herein, can be used to protect rabbits, rodents, birds, horses, cattle, and humans, including infant humans, from botulism, or from one or more of the symptoms of botulism, such as diarrheal disease, paralysis (either mild or severe), or death.

Toxin and toxin fragments can also be used to prepare compositions comprising neutralizing antibodies that immunoreact with the wild-type toxin. The resulting antisera can be used for the manufacture of a medicament for treating exposure to clostridial neurotoxin. Thus, antibody compositions, such as the isolated antisera or antibodies purified therefrom, can be used as a passive immune serum to prevent or treat botulism in patients exposed to the wild-type toxin. In such cases, the patient is a human, including an infant, suspected of having come in contact with the toxin, or is a human, including an infant, who has had known contact with the toxin, but is not yet showing symptoms of exposure. The antibody composition can also be used in a method of treating to ameliorate symptoms in patients that are suffering from the presence of toxin in their body. When the toxin is a clostridial neurotoxin, the symptoms include diarrhea and paralysis.

Methods of preparing passive immune sera are known in the art. For example, a vaccine composition can be administered to an animal such as a horse or a human until a neutralizing antibody response to wild type toxin is generated. Neutralizing antibodies can then be harvested, purified, and administered to patients exposed to, or exhibiting symptoms of contact with, the toxin to thereby treat or prevent botulism. In some cases, the antibodies are not purified after harvesting. When the neutralizing antibodies are from humans, the antibody preparation will generally be free of viruses, such as HIV and hepatitis. Methods of preparing human antisera are known in the art, and include the methods used to prepare IVIg. The neutralizing antibodies can be administered intravenously, intramuscularly, intradermally, or subcutaneously. Antibiotic therapy can be used in conjunction. Dosages for neutralizing antibodies generally vary from about 1 mg to 1000 mg/kg. Often, they are administered at a dosage of about 50-200 mg/kg of body weight.

The invention will be further clarified by the following examples, which are intended to be purely exemplary of the invention and in no way limiting.

EXAMPLES Example 1 Site-Directed Mutagenesis of LH_(N)/E to Remove One or More Cysteine Residues

Endopeptidase-ablating mutations (E213Q and H216Y relative to SEQ ID NO: 1 and SEQ ID NO: 2) were introduced into the LH_(N)/E coding sequence and the resulting cassettes cloned into plasmid vector pET26b. Various E. coli host strains were transformed and assessed for the ability to direct expression of a rLH_(N)/E fragment. While high levels of target protein could be produced, recombinant LH_(N)/E was expressed in all hosts as high molecular mass aggregate (FIGS. 1A and 1B). Those SDS-PAGE and gel filtration studies conducted under reducing and non-reducing conditions showed that LH_(N)/E aggregation results, at least in part, from intermolecular disulfide bond formation.

It was hypothesized that aggregation could be due to the formation of cysteine-linked disulfide bonds between multiple LH_(N)/E polypeptides. Molecular biology approaches were pursued to increase expression of soluble, non-aggregated rLH_(N)/E protein. Using computational analyses of the BoNT/E catalytic domain crystal structure two surface-proximal cysteine residues (Cys26 and Cys347 in SEQ ID NO: 1 and SEQ ID NO: 2) have been identified that most likely participate in intermolecular disulfide-bond-mediated bridging. Those residues were targeted for mutagenesis, and the aggregation properties of the mutated proteins were assessed.

LH_(N)/E was cloned into the expression vector pET26b (Novagen) and this plasmid clone was used for the mutagenesis procedure. Specifically, site directed mutagenesis (QuikChange II XL site-directed mutagenesis kit, Stratagene) was used to introduce two point mutations into the LH_(N)/E gene that change codons 26 and 347 (relative to a nucleic acid sequence encoding SEQ ID NO: 1 or SEQ ID NO: 2) from cysteine to structurally similar serine. While it is preferable to substitute the cysteine residue with a structurally similar amino acid, any amino acid may be substituted as long as that amino acid is incapable of forming an intermolecular disulfide bond.

The primer names and sequences used for mutagenesis are shown, with the nucleotides responsible for the cysteine to serine changes underlined. For both mutations, a TGC codon (cysteine) was changed to an AGC codon (serine). These two primers were used for the C26S mutation: C26S-LhnEfor: 5′-GTATATTAAACCGGGCGGCAGCCAGGAGTTTTATAAA AGC-3′ (SEQ ID NO: 3) and C26S-LhnErev: 5′-GCTTTTATAAAACTCCTGG CTGCCGCCCGGTTTAATATAC-3′ (SEQ ID NO: 4). These two primers were used for the C347S mutation: C347S-LhnEfor: 5′-GTACCAAATTTCAGGTGA AGAGCCGCCAAACCTACATCG-3′ (SEQ ID NO: 5) and C347S-LhnErev: 5′-CGATGTAGGTTTGGCGGCTCTTCACCTGAAATTTGGTAC-3′ (SEQ ID NO: 6).

Clones of pET26b/LH_(N)/E containing each single point mutation and both point mutations were made. The C26S single mutant, C347S single mutant, and C26S/C347S double mutant clones were expressed and analyzed for disulfide bond-mediated aggregation. As shown in FIGS. 2A and 2B, analysis of reduced and non-reduced samples revealed that intermolecular disulfide bonding was abolished in each of the LH_(N)/E clones (C26S single mutant, C347S single mutant, and C26S, C347S double mutant), whereas intermolecular disulfide bond formation was observable for the parental LH_(N)/E clone lacking the serine substitutions.

Example 2 Extending the LH_(N)/E Fragment with H_(c) Sequence Improves Solubility

The solubility of clostridial neurotoxin proteins can also be enhanced by creating proteins in which an LH_(N) domain, or a fragment of an LH_(N) domain, is expressed along with amino acid sequence from an Hc domain.

Recombinant truncated forms of the botulinum serotype E toxin, such as the LH_(N) fragments, have proven difficult to produce (express) and purify due to low solubility. Even at low concentrations, insoluble forms are often expressed in a non-native multimeric and aggregated state which renders them poor immunogens and unable to elicit protective levels of toxin neutralizing antibodies. To address this issue and enable the production of soluble (and possibly monomeric) protein, recombinant derivatives of the LH_(N)/E protein have been produced that carry various lengths of the adjoining Hc domain.

The following expression constructs were tested for protein solubility in the E. coli strain ER2566: LH_(N)/E; LH_(N)/E-Hc103; LH_(N)/E-Hc202; LH_(N)/E-Hc304; and LH_(N)/E-Hc406. Fifteen milliliters of LB media containing kanamycin (30 μg/mL) were inoculated with each strain containing the construct listed above. Inoculations were made directly from frozen glycerol stocks. These cultures grew at 37° C. overnight with shaking. The next morning, the overnight cultures were diluted into 1 L of 2×YT containing kanamycin (30 μg/mL) (15 mL into IL of 2×YT) in Fernbach flasks. The cultures shook at 37° C. for three hours. OD₆₀₀ ranged from 0.7-0.9 for all of the cultures. The Fernbach flasks were moved into 20° C. incubators, IPTG was added to 1 mM final concentration, and the flasks shook at 20° C. for 4 hours.

The 1 L cultures were collected by centrifugation and cell pellets were resuspended in 200 ml of 50 mM Tris, pH 8.0, 25 mM EDTA, pH 8.0. The cell suspensions were disrupted using the microfluidizer. Thirty-five milliliters of each cell lysate was centrifuged at 10,000×g for 30 minutes. The supernatants containing soluble protein were transferred into clean tubes and the insoluble pellets were resuspended in 35 mL of 50 mM Tris, pH 8.0, 25 mM EDTA, pH 8.0.

Equal volumes of total cell lysate, and soluble and insoluble fractions, were prepared for SDS-PAGE by the addition of sample buffer and boiling for 5 minutes. Equal amounts of each sample were subjected to SDS-PAGE. One set of gels was stained using MicroWave Blue reagent. Another set was transferred to PVDF membrane and subjected to western blotting using antisera specific for BoNT/E obtained from the Health Protection Agency.

The LH_(N)/E solubility is enhanced with the addition of amino acid residues from the Hc domain. This can be seen by comparing the amount of LH_(N)/E-Hc in soluble versus insoluble fractions in the Coomassie stained gels of FIG. 3 and the western blots of FIG. 4. LH_(N)/E, which is devoid of any Hc sequence, is detected predominately in the insoluble fraction. This is also observed for LH_(N)/E-Hc103 and LH_(N)/E-Hc202. However, the solubility of recombinant proteins containing longer segments of the Hc domains is greatly enhanced. This can be seen for LH_(N)/E-Hc406, which fractionates predominately with the soluble fraction, and also with LH_(N)/E-Hc304, which also displays enhanced solubility. These conclusions were confirmed by densitometry scans of the Coomassie stained gel.

We also compared the effect of treating LH_(N)/E and LH_(N)/E-Hc406 with the reducing agent DTT. FIG. 5A shows a Coomassie stained gel and FIG. 5B a western blot of the DTT treated (+DTT) and untreated (−DTT) samples. In both the presence and absence of DTT, more LH_(N)/E-Hc406 was found in the soluble (S) than in the insoluble (I) fraction.

The addition of H_(c) sequence to the LH_(N)/E fragment improves its solubility, as does the replacement of Cys 26 and Cys 347 with serine residues. We have also prepared expression constructs in which we combined these approaches. Following induction of protein expression, the pellet was harvested, then lysed and microfluidized. The lysate was separated into soluble and insoluble fractions by centrifugation. The levels of protein in the total lysate, soluble fraction, and insoluble fraction compared by running on a gel and western blotting with the anti-BoNT/E antisera. As shown in FIG. 6, the LH_(N)/E-Hc406 (C26S, C347S) mutant, like the LH_(N)/E (C26S, C347S) mutant, partitions predominantly to the soluble fraction.

Example 3 Immunogenicity of LH_(N)/E Cys to Ser Fragments and LH_(N)/E-Hc Fragments

Abolishing the ability of LH_(N)/E to form aberrant intermolecular disulfide bonds by replacing cysteine residues with amino acids that do not form disulfide bonds and extending the LH_(N)/E fragment with H_(c) sequence are two techniques that improve the yield of monomeric or less aggregated protein. These modifications will enhance the immunogenicity and protective efficacy of the LH_(N)/E fragment and the enzymatic activity of non-endopeptidase ablated toxins and toxin subfragments.

Immunogenicity of the recombinant proteins is tested in mice. Mice are immunized either with 10 μg of a LH_(N)/E protein in which one or more cysteine residues has been replaced with another amino acid that does not form disulfide bonds, with 10 μg of a LH_(N)/E protein that has been extended by inclusion of H_(c) sequence, with 10 μg of inactivated BoNT/E, or with other proteins described in the Examples. The proteins are suspended in an adjuvant emulsion. Control mice are immunized with saline emulsified in adjuvant for use as negative controls. The mice are immunized i.p. four times at 2-week intervals. One week after the last immunization, the mice are bled and the serum is analyzed by immunoblot for the presence of specific antibody. ELISA is used to determine the titer of the antisera. Two weeks after the last immunization, each mouse is challenged i.p. with 2 lethal doses of BoNT/E. Four days after challenge, the mice are scored for survivors.

Example 4 Amino Acid Sequences Encoded by Certain Constructs

The following amino acid sequences are encoded by constructs in which the type E neurotoxin is from Clostridium botulinum. In the sequences, the mutated cysteine residues, which have been substituted with serine residues, are indicated in bold and underline.

1. LH_(N)/E (endopeptidase active):

(SEQ ID NO: 7) PKINSFNYNDPVNDRTILYIKPGGSQEFYKSFNIMKNIWIIPERNVIGTT PQDFHPPTSLKNGDSSYYDPNYLQSDEEKDRFLKIVTKIFNRINNNLSGG ILLEELSKANPYLGNDNTPDNQFHIGDASAVEIKFSNGSQDILLPNVIIM GAEPDLFETNSSNISLRNNYMPSNHRFGSIAIVTFSPEYSFRFNDNCMNE FIQDPALTLMHELIHSLHGLYGAKGITTKYTITQKQNPLITNIRGTNIEE FLTFGGTDLNIITSAQSNDIYTNLLADYKKIASKLSKVQVSNPLLNPYKD VFEAKYGLDKDASGIYSVNINKFNDIFKKLYSFTEFDLRTKFQVKSRQTY IGQYKYFKLSNLLNDSIYNISEGYNINNLKVNFRGQNANLNPRIITPITG RGLVKKIIRFCKNIVSVKGIRKSICIEINNGELFFVASENSYNDDNINTP KEIDDTVTSNNNYENDLDQVILNFNSESAPGLSDEKLNLTIQNDAYIPKY DSNGTSDIEQHDVNELNVFFYLDAQKVPEGENNVNLTSSIDTALLEQPKI YTFFSSEFINNVNKPVQAALFVSWIQQVLVDFTTEANQKSTVDKIADISI VVPYIGLALNIGNEAQKGNFKDALELLGAGILLEFEPELLIPTILVFTIK SFLGSSDNKNKVIKAINNALKERDEKWKEVYSFIVSNWMTKINTQFNKRK EQMYQALQNQVNAIKTIIESKYNSYTLEEKNELTNKYDIKQIENELNQKV SIANNNIDRFLTESSISYLMKIINEVKINKLREYDENVKTYLLNYIIQHG SILGESQQELNSMVTDTLNNSIPFKLSSYTDDKILISYFNKFFK.

2. LH_(N)/E (endopeptidase attenuated):

(SEQ ID NO: 8) PKINSFNYNDPVNDRTILYIKPGGSQEFYKSFNIMKNIWIIPERNVIGTT PQDFHPPTSLKNGDSSYYDPNYLQSDEEKDRFLKIVTKIFNRINNNLSGG ILLEELSKANPYLGNDNTPDNQFHIGDASAVEIKFSNGSQDILLPNVIIM CAEPDLFETNSSNISLRNNYMPSNHRFGSIAIVTFSPEYSFRFNDNCMNE FIQDPALTLMHQLIYSLHGLYGAKGITTKYTITQKQNPLITNIRGTNIEE FLTFGGTDLNIITSAQSNDIYTNLLADYKKIASKLSKVQVSNPLLNPYKD VFEAKYGLDKDASGIYSVNINKFNDIFKKLYSFTEFDLRTKFQVKSRQTY IGQYKYFKLSNLLNDSIYNISEGYNINNLKVNFRGQNANLNPRIITPITG RGLVKKIIRFCKNIVSVKGIRKSICIEINNGELFFVASENSYNDDNINTP KEIDDTVTSNNNYENDLDQVILNFNSESAPGLSDEKLNLTIQNDAYIPKY DSNGTSDIEQHDVNELNVFFYLDAQKVPEGENNVNLTSSIDTALLEQPKI YTFFSSEFINNVNKPVQAALFVSWIQQVLVDFTTEANQKSTVDKIADISI VVPYIGLALNIGNEAQKGNFKDALELLGAGILLEFEPELLIPTILVFTIK SFLGSSDNKNKVIKAINNALKERDEKWKEVYSFIVSNWMTKINTQFNKRK EQMYQALQNQVNAIKTIIESKYNSYTLEEKNELTNKYDIKQIENELNQKV SIANNNIDRFLTESSISYLMKIINEVKINKLREYDENVKTYLLNYIIQHG SILGESQQELNSMVTDTLNNSIPFKLSSYTDDKILISYFNKFFK.

3. BoNT/E neurotoxin (endopeptidase attenuated):

(SEQ ID NO: 9) PKINSFNYNDPVNDRTILYIKPGGSQEFYKSFNIMKNIWIIPERNVIGTT PQDFHPPTSLKNGDSSYYDPNYLQSDEEKDRFLKIVTKIFNRINNNLSGG ILLEELSKANPYLGNDNTPDNQFHIGDASAVEIKFSNGSQDILLPNVIIM GAEPDLFETNSSNISLRNNYMPSNHRFGSIAIVTFSPEYSFRFNDNCMNE FIQDPALTLMHQLIYSLHGLYGAKGITTKYTITQKQNPLITNIRGTNIEE FLTFGGTDLNIITSAQSNDIYTNLLADYKKIASKLSKVQVSNPLLNPYKD VFEAKYGLDKDASGIYSVNINKFNDIFKKLYSFTEFDLRTKFQVKSRQTY IGQYKYFKLSNLLNDSIYNISEGYNINNLKVNFRGQNANLNPRIITPITG RGLVKKIIRFCKNIVSVKGIRKSICIEINNGELFFVASENSYNDDNINTP KEIDDTVTSNNNYENDLDQVILNFNSESAPGLSDEKLNLTIQNDAYIPKY DSNGTSDIEQHDVNELNVFFYLDAQKVPEGENNVNLTSSIDTALLEQPKI YTFFSSEFINNVNKPVQAALFVSWIQQVLVDFTTEANQKSTVDKIADISI VVPYIGLALNIGNEAQKGNFKDALELLGAGILLEFEPELLIPTILVFTIK SFLGSSDNKNKVIKAINNALKERDEKWKEVYSFIVSNWMTKINTQFNKRK EQMYQALQNQVNAIKTIIESKYNSYTLEEKNELTNKYDIKQIENELNQKV SIAMNNIDRFLTESSISYLMKIINEVKINKLREYDENVKTYLLNYIIQHG SILGESQQELNSMVTDTLNNSIPFKLSSYTDDKILISYFNKFFKRIKSSS VLNMRYKNDKYVDTSGYDSNININGDVYKYPTNKNQFGIYNDKLSEVNIS QNDYIIYDNKYKNFSISFWVRIPNYDNKIVNVNNEYTIINCMRDNNSGWK VSLNHNEIIWTFEDNRGINQKLAFNYGNANGISDYINKWIFVTITNDRLG DSKLYINGNLIDQKSILNLGNIHVSDNILFKIVNCSYTRYIGIRYFNIFD KELDETEIQTLYSNEPNTNILKDFWGNYLLYDKEYYLLNVLKPNNFIDRR KDSTLSINNIRSTILLANRLYSGIKVKIQRVNNSSTNDNLVRKNDQVYIN FVASKTHLFPLYADTATTNKEKTIKISSSGNRFNQVVVMNSVGNCTMNFK NNNGNNIGLLGFKADTVVASTLFYTHMRDHTNSNGCFWNFISEEHGWQE K.

4. Extended LH_(N)/E neurotoxin (endopeptidase attenuated):

(SEQ ID NO: 10) PKINSFNYNDPVNDRTILYIKPGGSQEFYKSFNIMKNIWIIPERNVIGTT PQDFHPPTSLKNGDSSYYDPNYLQSDEEKDRFLKIVTKIFNRINNNLSGG ILLEELSKANPYLGNDNTPDNQFHIGDASAVEIKFSNGSQDILLPNVIIM GAEPDLFETNSSNISLRNNYMPSNHRFCSIAIVTFSPEYSFRFNDNCMNE FIQDPALTLMHQLIYSLHGLYGAKGITTKYTITQKQNPLITNIRGTNIEE FLTFGGTDLNIITSAQSNDIYTNLLADYKKIASKLSKVQVSNPLLNPYKD VFEAKYGLDKDASGIYSVNINKFNDIFKKLYSFTEFDLRTKFQVKSRQTY IGQYKYFKLSNLLNDSIYNISEGYNINNLKVNFRGQNANLNPRIITPITG RGLVKKIIRFCKNIVSVKGIRKSICIEINNGELFFVASENSYNDDNINTP KEIDDTVTSNNNYENDLDQVILNFNSESAPGLSDEKLNLTIQNDAYIPKY DSNGTSDIEQHDVNELNVFFYLDAQKVPEGENNVNLTSSIDTALLEQPKI YTFFSSEFINNVNKPVQAALFVSWIQQVLVDFTTEANQKSTVDKIADISI VVPYIGLALNIGNEAQKGNFKDALELLGAGILLEFEPELLIPTILVFTIK SFLGSSDNKNKVIKAINNALKERDEKWKEVYSFIVSNWMTKINTQFNKRK EQMYQALQNQVNAIKTIIESKYNSYTLEEKNELTNKYDIKQIENELNQKV SIANNNIDRFLTESSISYLMKIINEVKINKLREYDENVKTYLLNYIIQHG SILGESQQELNSMVTDTLNNSIPFKLSSYTDDKILISYFNKFFKRIKSSS VLNMRYKNDKYVDTSGYDSNININGDVYKYPTNKNQFGIYNDKLSEVNIS QNDYIIYDNKYKNFSISFWVRIPNYDNKIVNVNNEYTIINCMRDNNSGWK VSLNHNEIIWTFEDNRGINQKLAFNYGNANGISDYINKWIFVTITNDRLG DSKLYINGNLIDQKSILNLGNIHVSDNILFKIVNCSYTRYIGIRYFNIFD KELDETEIQTLYSNE.

The following amino acid sequences are encoded by constructs in which the type E neurotoxin is from Clostridium butyricum. In the sequences, the mutated cysteine residues, which have been substituted with serine residues, are indicated in bold and underline.

5. LH_(N)/E (endopeptidase active):

(SEQ ID NO: 11) PTINSFNYNDPVNNRTILYIKPGGSQQFYKSFNIMKNIWIIPERNVIGTI PQDFLPPTSLKNGDSSYYDPNYLQSDQEKDKFLKIVTKIFNRINDNLSCR ILLEELSKANPYLGNDNTPDGDFIINDASAVPIQFSNGSQSILLPNVIIM GAEPDLFETNSSNISLRNNYMPSNHGFGSIAIVTFSPEYSFRFKDNSMNE FIQDPALTLMHELIHSLHGLYGAKGITTKYTITQKQNPLITNIRGTNIEE FLTFGGTDLNIITSAQSNDIYTNLLADYKKIASKLSKVQVSNPLLNPYKD VFEAKYGLDKDASGIYSVNINKFNDIFKKLYSFTEFDLATKFQVKSRQTY IGQYKYFKLSNLLNDSIYNISEGYNINNLKVNFRGQNANLNPRIITPITG RGLVKKIIRFCKNIVSVKGIRKSICIEINNGELFFVASENSYNDDNINTP KEIDDTVTSNNNYENDLDQVILNFNSESAPGLSDEKLNLTIQNDAYIPKY DSNGTSDIEQHDVNELNVFFYLDAQKVPEGENNVNLTSSIDTALLEQPKI YTFFSSEFINNVNKPVQAALFVGWIQQVLVDFTTEANQKSTVDKIADISI VVPYIGLALNIGNEAQKGNFKDALELLGAGILLEFEPELLIPTILVFTIK SFLGSSDNKNKVIKAINNALKERDEKWKEVYSFIVSNWMTKINTQFNKPK EQMYQALQNQVNALKAIIESKYNSYTLEEKNELTNKYDIEQIENELNQKV SIAMNNIDRFLTESSISYLMKLINEVKINKLREYDENVKTYLLDYIIKHG SILGESQQELNSMVIDTLNNSIPFKLSSYTDDKILISYFNKFFK.

6. LH_(N)/E (endopeptidase attenuated):

(SEQ ID NO: 12) PTINSFNYNDPVNNRTILYIKPGGSQQFYKSFNIMKNIWIIPERNVIGTI PQDFLPPTSLKNGDSSYYDPNYLQSDQEKDKFLKIVTKIFNRINDNLSGR ILLEELSKANPYLGNDNTPDGDFIINDASAVPIQFSNGSQSILLPNVIIM GAEPDLFETNSSNISLRNNYMPSNHGFGSIAIVTFSPEYSFRFKDNSMNE FIQDPALTLMHQLIYSLHGLYGAKGITTKYTITQKQNPLITNIRGTNIEE FLTFGGTDLNIITSAQSNDIYTNLLADYKKIASKLSKVQVSNPLLNPYKD VFEAKYGLDKDASGIYSVNINKFNDIFKKLYSFTEFDLATKFQVKSRQTY IGQYKYFKLSNLLNDSIYNISEGYNINNLKVNFRGQNANLNPRIITPITG RGLVKKIIRFCKNIVSVKGIRKSICIEINNGELFFVASSNSYNDDNINTP KEIDDTVTSNNNYENDLDQVILNFNSESAPGLSDEKLNLTIQNDAYIPKY DSNGTSDIEQHDVNELNVFFYLDAQKVPEGENNVNLTSSIDTALLEQPKI YTFFSSEFININNKPVQAALFVGWIQQVLVDFTTEANQKSTVDKIADISI VVPYIGLALNIGNEAQKGNFKDALELLGAGILLEFEPELLIPTILVFTIK SFLGSSDNKNKVIKAINNALKERDEKWKEVYSFIVSNWMTKINTQFNKRK EQMYQALQNQVNALKAIIESKYNSYTLEEKNELTNKYDIEQIENELNQKV SIAMNNIDRFLTESSISYLMKLINEVKINKLREYDENVKTYLLDYIIKHG SILGESQQELNSMVIDTLNNSIPFKLSSYTDDKILISYFNKFFK.

7. BoNT/E neurotoxin (endopeptidase attenuated):

(SEQ ID NO: 13) PTINSFNYNDPVNNRTILYIKPGGSQQFYKSFNIMKNIWIIPERNVIGTI PQDFLPPTSLKNGDSSYYDPNYLQSDQEKDKFLKIVTKIFNRINDNLSGR ILLEELSKANPYLGNDNTPDGDFIINDASAVPIQFSNGSQSILLPNVIIM GAEPDLFETNSSNISLRNNYMPSNHGFGSIAIVTFSPEYSFRFKDNSMNE FIQDPALTLMHQLIYSLHGLYGAKGITTKYTITQKQNPLITNIRGTNIEE FLTFGGTDLNIITSAQSNDIYTNLLADYKKIASKLSKVQVSNPLLNPYKD VFEAKYGLDKDASGIYSVNINKFNDIFKKLYSFTEFDLATKFQVKSRQTY IGQYKYFKLSNLLNDSIYNISEGYNINNLKVNFRGQNANLNPRIITPITG RGLVKKIIRFCKNIVSVKGIRKSICIEINKGELFFVASENSYNDDNINTP KEIDDTVTSNNNYENDLDQVILNFNSESAPGLSDEKLNLTIQNDAYIPKY DSNGTSDIEQHDVNELNVFFYLDAQKVPEGENNVNLTSSIDTALLEQPKI YTFFSSEFINNVNKPVQAALFVGWIQQVLVDFTTEANQKSTVDKIADISI VVPYIGLALNIGNEAQKGNFKDALELLGAGILLEFEPELLIPTILVFTIK SFLGSSDNKNKVIKAINNALKERDEKWKEVYSFIVSNWMTKINTQFNKRK EQMYQALQNQVNALKAIIESKYNSYTLEEKNELTNKYDIEQIENELNQKV SIANNNIDRFLTESSISYLMKLINEVKINKLREYDENVKTYLLDYIIKHG SILGESQQELNSMVIDTLNNSIPFKLSSYTDDKILISYFNKFFKRIKSSS VLNMRYKNDKYVDTSGYDSNININGDVYKYPTNKNQFGIYNDKLSEVNIS QNDYIIYDNKYKNFSISFWVRIPNYDNKIVNVNNEYTIINCMRDNNSGWK VSLNHNEIIWTLQDNSGINQKLAFNYGNANGISDYINKWIFVTITNDRLG DSKLYINGNLIDKKSILNLGNIHVSDNILFKIVNCSYTRYIGIRYFNIFD KELDETEIQTLYNNEPNANILKDFWGNYLLYDKEYYLLNVLKPNNFINRR TDSTLSINNIRSTILLANRLYSGIKVKIQRVNNSSTNDNLVRKNDQVYIN FVASKTHLLPLYADTATTNKEKTIKISSSGNRFNQVVVMNSVGNCTMNFK NNNGNNIGLLGFKADTVVASTLFYTHNRDNTNSNGFFWNFISEEHGWQE K.

8. Extended LH_(N)/E (endopeptidase attenuated):

(SEQ ID NO: 14) PKINSFNYNDPVNDRTILYIKPGGSQEFYKSFNIMKNIWIIPERNVIGTT PQDFHPPTSLKNGDSSYYDPNYLQSDEEKDRFLKIVTKIFNRINNNLSGG ILLEELSKANPYLGNDNTPDNQFHIGDASAVEIKFSNGSQDILLPNVIIM GAEPDLFETNSSNISLRNNYMPSNHRFGSIAIVTFSPEYSFRFNDNCMNE FIQDPALTLMHQLIYSLHGLYGAKGITTKYTITQKQNPLITNIRGTNIEE FLTFGGTDLNIITSAQSNDIYTNLLADYKKIASKLSKVQVSNPLLNPYKD VFEAKYGLDKDASGIYSVNINKFNDIFKKLYSFTEFDLRTKFQVKSRQTY IGQYKYFKLSNLLNDSIYNISEGYNINNLKVNFRGQNANLNPRIITPITG RGLVKKIIRFCKNIVSVKGIRKSICIEINNGELFFVASENSYNDDNINTP KEIDDTVTSNNNYENDLDQVILNFNSESAPGLSDEKLNLTIQNDAYIPKY DSNGTSDIEQHDVNELNVFFYLDAQKVPEGENNVNLTSSIDTALLEQPKI YTFFSSEFINNVNKPVQAALFVSWIQQVLVDFTTEANQKSTVDKIADISI VVPYIGLALNIGNEAQKGNFKDALELLGAGILLEFEPELLIPTILVFTIK SFLGSSDNKNKVIKAINNALKERDEKWKEVYSFIVSNWMTKINTQFNKRK EQMYQALQNQVNAIKTIIESKYNSYTLEEKNELTNKYDIKQIENELNQKV SIANNNIDRFLTESSISYLMKIINEVKINKLREYDENVKTYLLNYIIQHG SILGESQQELNSMVTDTLNNSIPFKLSSYTDDKILISYFNKFFKRIKSSS VLNMRYKNDKYVDTSGYDSNININGDVYKYPTNKNQFGIYNDKLSEVNIS QNDYIIYDNKYKNFSISFWVRIPNYDNKIVNVNNEYTIINCMRDNNSGWK VSLNHNEIIWTFEDNRGINQKLAFNYGNANGISDYINKWIFVTITNDRLG DSKLYINGNLIDQKSILNLGNIHVSDNILFKIVNCSYTRYIGIRYFNIFD KELDETEIQTLYSNE.

Other embodiments of the invention will be apparent to those skilled in the art from consideration of the specification and practice of the invention disclosed herein, such as, for example, C. botulinum neurotoxins of type A, B, C, D, F, or G mutated or truncated according to the method of the invention that exhibit improved solubility. It is intended that the specification and examples be considered as exemplary only, with the true scope and spirit of the invention being indicated by the following claims. 

1-34. (canceled)
 35. A recombinant protein comprising a truncated botulinum serotype E toxin, wherein the truncation improves the solubility of the recombinant protein.
 36. The protein of claim 35, wherein the truncation is in the Hc domain.
 37. The protein of claim 35, wherein the truncated protein comprises the LH_(N)/E domain and the amino terminal 103 amino acids of the Hc domain.
 38. The protein of claim 35, wherein the truncated protein comprises the amino terminal 948 amino acids of the serotype E toxin.
 39. The protein of claim 35, wherein the truncated protein comprises the LH_(N)/E domain and the amino terminal 202 amino acids of the Hc domain.
 40. The protein of claim 35, wherein the truncated protein comprises the amino terminal 1047 amino acids of the serotype E toxin.
 41. The protein of claim 35, wherein the truncated protein comprises the LH_(N)/E domain and the amino terminal 304 amino acids of the Hc domain.
 42. The protein of claim 35, wherein the truncated protein comprises the amino terminal 1149 amino acids of the serotype E toxin.
 43. A nucleic acid encoding a recombinant protein of claim
 35. 44. A method for improving the solubility of a clostridial neurotoxin, comprising: (a) providing a nucleic acid sequence encoding a clostridial neurotoxin; (b) modifying the nucleic acid sequence so that it encodes the LH_(N) fragment and a portion of the H_(c) fragment of the neurotoxin; (c) transforming the modified nucleic acid sequence into a host cell capable of expressing the modified nucleic acid sequence; and (d) expressing the modified nucleic acid sequence to produce the protein.
 45. A method of treating or preventing botulism comprising administering a protein of claim 35 to a patient in need thereof.
 46. A composition comprising a protein of claim 35 and a pharmaceutically acceptable carrier.
 47. A method of protecting an individual from botulism, comprising administering to the individual a composition of claim
 46. 48. A method of producing antibodies that neutralize a clostridial neurotoxin, comprising administering the composition of claim 46 to an animal, allowing the animal to develop neutralizing antibodies to the clostridial neurotoxin, and isolating an antiserum that neutralizes the clostridial neurotoxin from the animal.
 49. An antiserum produced by the method of claim
 48. 50. A method of treating exposure to a clostridial neurotoxin, comprising administering to a patient that has been exposed to the clostridial neurotoxin the antiserum of claim
 49. 51. A mutated botulinum serotype E toxin comprising either or both of a leucine residue substituted for the tryptophan residue at position 1223 and a phenylalanine residue for the tyrosine residue at position 1224 of SEQ ID NO: 1 or SEQ ID NO:
 2. 52. A method of treating or preventing botulism comprising administering a protein of claim 51 to a patient in need thereof. 53-58. (canceled) 